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体外糖皮质激素受体介导的骨骼肌细胞中谷氨酰胺合成酶的诱导作用

Glucocorticoid receptor-mediated induction of glutamine synthetase in skeletal muscle cells in vitro.

作者信息

Max S R, Thomas J W, Banner C, Vitkovic L, Konagaya M, Konagaya Y

出版信息

Endocrinology. 1987 Mar;120(3):1179-83. doi: 10.1210/endo-120-3-1179.

Abstract

We studied the regulation by glucocorticoids of glutamine synthetase in L6 muscle cells in culture. Glutamine synthetase activity was strikingly enhanced by dexamethasone. The dexamethasone-mediated induction of glutamine synthetase activity was blocked by RU38486 [11 beta-(4-dimethylaminophenyl)17 beta-hydroxy-17 alpha-(prop-1-ynyl)estra-4,9-dien-3-one], a glucocorticoid antagonist, indicating the involvement of intracellular glucocorticoid receptors in the induction process. RU38486 alone was without effect. Northern blot analysis revealed that dexamethasone-mediated enhancement of glutamine synthetase activity involves increased levels of glutamine synthetase mRNA. Increased enzyme activity was specific for glucocorticoids; other steroid hormones were essentially without effect. The induction of glutamine synthetase was selective, in that glutaminase activity was not induced by dexamethasone treatment of L6 cells. Thus, glucocorticoids regulate the expression of glutamine synthetase mRNA in cultured muscle cells via interaction with intracellular receptors. Such regulation may be relevant to control of glutamine production by muscle.

摘要

我们研究了培养的L6肌细胞中糖皮质激素对谷氨酰胺合成酶的调控作用。地塞米松显著增强了谷氨酰胺合成酶的活性。糖皮质激素拮抗剂RU38486 [11β-(4-二甲基氨基苯基)-17β-羟基-17α-(丙-1-炔基)雌甾-4,9-二烯-3-酮] 可阻断地塞米松介导的谷氨酰胺合成酶活性诱导,表明细胞内糖皮质激素受体参与了诱导过程。单独使用RU38486没有效果。Northern印迹分析显示,地塞米松介导的谷氨酰胺合成酶活性增强涉及谷氨酰胺合成酶mRNA水平的增加。酶活性的增加对糖皮质激素具有特异性;其他类固醇激素基本没有作用。谷氨酰胺合成酶的诱导具有选择性,因为用地塞米松处理L6细胞不会诱导谷氨酰胺酶活性。因此,糖皮质激素通过与细胞内受体相互作用来调节培养肌细胞中谷氨酰胺合成酶mRNA的表达。这种调节可能与肌肉中谷氨酰胺产生的控制有关。

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